104220-97-5Relevant articles and documents
A ROUTE TO PROSTAGLANDIN PRECURSORS FROM 1-(PHENYLTHIO)-2-OCTENYLLITHIUM.
Binns, Malcolm R.,Haynes, Richard K.,Lambert, Dale E.,Schober, Paul A.
, p. 3385 - 3388 (2007/10/02)
The enolates generated by the conjugate addition of 1-(phenylthio)-2-octenyllithium to 4-tert-butoxycyclopent-2-en-1-one and γ-crotonolactone react with methyl 7-halohept-5-ynoates in the presence of Ph3SnCl to deliver products which may be converted into prostaglandin precursors.